Evidence map›Paper›PMID 39683510›Full record

SynthesisNutrients2024

Efficacy of Zinc Supplementation in the Management of Primary Dysmenorrhea: A Systematic Review and Meta-Analysis.

Ting-Jui Hsu, Rong-Hong Hsieh, Chin-Huan Huang, Chih-Shou Chen, Wei-Yu Lin, Yun-Ching Huang, Jian-Hui Lin, Kuo-Tsai Huang, Yu-Liang Liu, Hui-Ming Tsai and 1 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ting-Jui HsuDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.ORCID 0009-0004-4453-9590
Rong-Hong HsiehSchool of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 11031, Taiwan.
Chin-Huan HuangDepartment of Nutrition Therapy, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chiayi 622401, Taiwan.
Chih-Shou ChenDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.ORCID 0000-0002-5785-2373
Wei-Yu LinDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
Yun-Ching HuangDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
Jian-Hui LinDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
Kuo-Tsai HuangDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
Yu-Liang LiuDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.
Hui-Ming TsaiSchool of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 11031, Taiwan.ORCID 0009-0001-8382-0017
Dong-Ru HoDivision of Urology, Department of Surgery, Chang Gung Memorial Hospital, Chiayi 61363, Taiwan.ORCID 0000-0002-1805-0538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesPrimary dysmenorrhea (PD) is a common condition affecting up to 90% of menstruating women, which often results in significant pain without an underlying pathology. Zinc, recognized for its anti-inflammatory and antioxidant effects through inhibiting prostaglandin production and superoxide dismutase 1 (SOD1) upregulation, alleviates menstrual pain by preventing uterine spasms and enhancing microcirculation in the endometrium, suggesting its potential as an alternative treatment for primary dysmenorrhea. The goal of this systematic review and meta-analysis was to assess the efficacy and safety of zinc supplementation in reducing pain severity among women with PD and to explore the influence of dosage and treatment duration.

methodsFollowing the PRISMA 2020 guidelines, we conducted an extensive search across databases such as PubMed, Embase, Cochrane Library, Web of Science, and Google Scholar, up to May 2024. Randomized controlled trials assessing the effects of zinc supplementation on pain severity in women with PD were included. Pain severity was evaluated with established tools, such as the Visual Analog Scale (VAS). Risk of bias was assessed using the Cochrane Risk of Bias 2 (RoB2) tool. Two reviewers independently performed the data extraction, and a random-effects model was used for meta-analysis. Meta-regressions were conducted to examine the influence of zinc dosage and treatment duration on pain reduction. Adverse events were also analyzed.

resultsSix RCTs involving 739 participants met the inclusion criteria. Zinc supplementation significantly reduced pain severity compared to placebo (Hedges's g = -1.541; 95% CI: -2.268 to -0.814;

conclusionsZinc supplementation is an effective and well-tolerated option for reducing pain severity in women with primary dysmenorrhea. Doses as low as 7 mg/day of elemental zinc are sufficient to achieve significant pain relief, with longer durations (≥8 weeks) enhancing efficacy. The favorable safety profile and ease of use support the consideration of zinc supplementation as a practical approach to managing primary dysmenorrhea.

Indexed as

Dietary SupplementsDysmenorrheaZincFemaleHumansPain MeasurementRandomized Controlled Trials as TopicTreatment OutcomeZincanti-inflammatorymenstrual painmeta-analysisnutritional supplementspain reliefprimary dysmenorrhearandomized controlled trialswomen’s healthzinc supplementation

Identifiers

PMID39683510
PMCPMC11643716

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.